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MAURIZIO AVERNA

Curriculum and Research

AVERNA MAURIZIO

MAURIZIO AVERNA

 

Promozione della Salute, Materno-Infantile, di Medicina Interna e Specialistica di Eccellenza “G. D’Alessandro”

Contacts

maurizio.averna@unipa.it

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Publications

Date Title Type Record
2024 Familial hypercholesterolaemia in children and adolescents from 48 countries: a cross-sectional study Articolo in rivista Go to
2024 Do genetically determined very high and very low LDL levels contribute to Lp(a) plasma concentration? Articolo in rivista Go to
2024 Derivation and validation of a predictive mortality model of in-hospital patients with Acinetobacter baumannii nosocomial infection or colonization Articolo in rivista Go to
2024 Six genetic variants are associated with cardiovascular disease independently from canonical risk factors: a new method to refine GWAS results based on the UKBiobank phenotype database Articolo in rivista Go to
2024 Erdheim-Chester disease as complex clinical presentation and diagnosis: A case report and concise review of literature Articolo in rivista Go to
2024 Consensus document on diagnosis and management of familial hypercholesterolemia from the Italian Society for the Study of Atherosclerosis (SISA) Articolo in rivista Go to
2023 Statin-induced autoimmune myositis: a proposal of an "experience-based" diagnostic algorithm from the analysis of 69 patients Articolo in rivista Go to
2023 Lipoprotein(a) Genotype Influences the Clinical Diagnosis of Familial Hypercholesterolemia Articolo in rivista Go to
2023 Novel LDL-cholesterol lowering therapies: A step forward a personalized medicine Nota o commento Go to
2023 Consensus document on Lipoprotein(a) from the Italian Society for the Study of Atherosclerosis (SISA) Articolo in rivista Go to
2023 Long-term hepatic safety of lomitapide in homozygous familial hypercholesterolaemia Articolo in rivista Go to
2023 Refinement of the diagnostic approach for the identification of children and adolescents affected by familial hypercholesterolemia: Evidence from the LIPIGEN study Articolo in rivista Go to
2023 APOC-III: a Gatekeeper in Controlling Triglyceride Metabolism Review essay (rassegna critica) Go to
2022 Worldwide experience of homozygous familial hypercholesterolaemia: retrospective cohort study Articolo in rivista Go to
2022 Diagnosis of familial hypercholesterolemia in a large cohort of Italian genotyped hypercholesterolemic patients Articolo in rivista Go to
2022 Twelve Variants Polygenic Score for Low-Density Lipoprotein Cholesterol Distribution in a Large Cohort of Patients With Clinically Diagnosed Familial Hypercholesterolemia With or Without Causative Mutations Articolo in rivista Go to
2022 Lifestyle versus ezetimibe plus lifestyle in patients with biopsy-proven non-alcoholic steatohepatitis (LISTEN): A double-blind randomised placebo-controlled trial Articolo in rivista Go to
2022 Lp(a): a genetic cause of clinical FH in children Nota o commento Go to
2022 Clinical evaluation of bempedoic acid for the treatment of hyperlipidaemia Articolo in rivista Go to
2022 A subgroup analysis of the ODYSSEY APPRISE study: Safety and efficacy of alirocumab in the Italian cohort Articolo in rivista Go to
2022 Efficacy of Long-Term Treatment of Autosomal Recessive Hypercholesterolemia With Lomitapide: A Subanalysis of the Pan-European Lomitapide Study Articolo in rivista Go to
2022 Comparison of two polygenic risk score to identify non-monogenic primary hypocholesterolemias in a large cohort of Italian hypocholesterolemic subjects: Polygenic hypocholesterolemias Articolo in rivista Go to
2022 Effects of PCSK9 inhibitors on HDL cholesterol efflux and serum cholesterol loading capacity in familial hypercholesterolemia subjects: a multi-lipid-center real-world evaluation Articolo in rivista Go to
2022 An unusual case of chronic diarrhea: a case report Articolo in rivista Go to
2022 Efficacy and safety of lomitapide in familial chylomicronaemia syndrome Articolo in rivista Go to
2021 EFFECTIVENESS AND SAFETY OF LOMITAPIDE IN A PATIENT WITH FAMILIAL CHYLOMICRONEMIA SYNDROME Abstract in atti di convegno pubblicato in rivista Go to
2021 Practical guidance for combination lipid-modifying therapy in high- and very-high-risk patients: A statement from a European Atherosclerosis Society Task Force Articolo in rivista Go to
2021 Lack of phenotypic additive effect of familial defective apolipoprotein B3531 in familial hypercholesterolaemia Articolo in rivista Go to
2021 EFFICACY AND SAFETY OF LOMITAPIDE IN HOMOZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA: THE PAN-EUROPEAN RETROSPECTIVE OBSERVATIONAL STUDY Articolo in rivista Go to
2021 Global perspective of familial hypercholesterolaemia: a cross-sectional study from the EAS Familial Hypercholesterolaemia Studies Collaboration (FHSC) Articolo in rivista Go to
2021 Resistive index of ophthalmic artery as an imaging biomarker of hypertension-related vascular and kidney damage Articolo in rivista Go to
2021 Hyperalphalipoproteinemia and Beyond: The Role of HDL in Cardiovascular Diseases Review essay (rassegna critica) Go to
2021 Effectiveness and safety of lomitapide in a patient with familial chylomicronemia syndrome Articolo in rivista Go to
2021 DeepSRE: Identification of sterol responsive elements and nuclear transcription factors Y proximity in human DNA by Convolutional Neural Network analysis Articolo in rivista Go to
2021 Long-term efficacy of lipoprotein apheresis and lomitapide in the treatment of homozygous familial hypercholesterolemia (HoFH): a cross-national retrospective survey Articolo in rivista Go to
2021 rs629301 CELSR2 polymorphism confers a ten-year equivalent risk of critical stenosis assessed by coronary angiography Articolo in rivista Go to
2021 Lomitapide does not alter PCSK9 and Lp(a) levels in homozygous familial hypercholesterolemia patients: Analysis on cytokines and lipid profile Articolo in rivista Go to
2021 Lipoprotein abnormalities in chronic kidney disease and renal transplantation Review essay (rassegna critica) Go to
2021 One year after the ESC/EAS guidelines on cholesterol control. What's the new evidence? What's missing? Review essay (rassegna critica) Go to
2020 MOLECULAR CHARACTERIZATION OF PATIENTS WITH AND WITHOUT CORONARY ARTERY DISEASE WITH "EXTREME LDL-C PHENOTYPES" Abstract in atti di convegno pubblicato in rivista Go to
2020 PCSK9-D374Y MEDIATED LDL-R DEGRADATION CAN BE FUNCTIONALLY INHIBITED BY EGF-A AND TRUNCATED EGF-A PEPTIDES. AN IN VITRO STUDY Abstract in atti di convegno pubblicato in rivista Go to
2020 Appropriateness criteria for the management of lipid-lowering therapy with alirocumab in high cardiovascular risk patients. The opinion of a multidisciplinary group of Italian experts Articolo in rivista Go to
2020 MUTATION IN CANDIDATE GENES ACCOUNT FOR A SMALL MINORITY OF HYPOBETALIPOPROTEINEMIAS AND NGS ANALYSIS SUPPORT POLYGENICITY IN MUTATION-NEGATIVE PATIENTS Abstract in atti di convegno pubblicato in rivista Go to
2020 Homozygous familial hypercholesterolemia in Italy: Clinical and molecular features Articolo in rivista Go to
2020 Rapid degradation of ABCA1 protein following cAMP withdrawal and treatment with PKA inhibitor suggests ABCA1 is a short-lived protein primarily regulated at the transcriptional level Articolo in rivista Go to
2020 PCSK9-D374Y mediated LDL-R degradation can be functionally inhibited by EGF-A and truncated EGF-A peptides: An in vitro study Articolo in rivista Go to
2020 Reported muscle symptoms during statin treatment amongst Italian dyslipidaemic patients in the real-life setting: the PROSISA Study Articolo in rivista Go to
2020 Reported muscle symptoms during statin treatment amongst Italian dyslipidaemic patients in the real-life setting: the PROSISA Study Articolo in rivista Go to
2020 Genetically determined hypercholesterolaemia results into premature leucocyte telomere length shortening and reduced haematopoietic precursors Articolo in rivista Go to
2020 Therapeutic options for homozygous familial hypercholesterolemia: the role of Lomitapide Articolo in rivista Go to
2020 Rare dyslipidaemias, from phenotype to genotype to management: a European Atherosclerosis Society task force consensus statement Review essay (rassegna critica) Go to
2020 NPC1L1 and ABCG5/8 induction explain synergistic fecal cholesterol excretion in ob/ob mice co-treated with PPAR-α and LXR agonists Articolo in rivista Go to
2019 PREVALENCE OF STATIN INTOLERANCE IN A COHORT OF OUTPATIENTS IN A LIPID CLINIC Abstract in atti di convegno pubblicato in rivista Go to
2019 IDENTIFICATION OF P.LEU167DEL APOE GENE MUTATION BY NEXT GENERATION SEQUENCING IN A LARGE HYPERCHOLESTEROLEMIC FAMILY Abstract in atti di convegno pubblicato in rivista Go to
2019 Resting energy expenditure and substrate oxidation in malnourished patients with type 1 glycogenosis Articolo in rivista Go to
2019 Polyvascular subclinical atherosclerosis in familial hypercholesterolemia: The role of cholesterol burden and gender Articolo in rivista Go to
2019 Is echocardiography mandatory for patients with chronic kidney disease? Articolo in rivista Go to
2019 Treatment effect of alirocumab according to age group, smoking status, and hypertension: Pooled analysis from 10 randomized ODYSSEY studies Articolo in rivista Go to
2019 Relationship of a Body Shape Index and Body Roundness Index with carotid atherosclerosis in arterial hypertension Articolo in rivista Go to
2018 An irregular atrial tachycardia : What is the underlying mechanism? Recensione in rivista Go to
2018 Genetic epidemiology of autosomal recessive hypercholesterolemia in Sicily: Identification by next-generation sequencing of a new kindred Articolo in rivista Go to
2018 Autosomal Recessive Hypercholesterolemia: Long-Term Cardiovascular Outcomes Articolo in rivista Go to
2018 Major adverse cardiovascular events in non-valvular atrial fibrillation with chronic obstructive pulmonary disease: the ARAPACIS study Articolo in rivista Go to
2018 Statin utilization and lipid goal attainment in high or very-high cardiovascular risk patients: Insights from Italian general practice Articolo in rivista Go to
2018 Lipoprotein-associated phospholipase A2 activity is increased in patients with definite familial hypercholesterolemia compared with other forms of hypercholesterolemia Articolo in rivista Go to
2018 Diabetes and aortic root dimension: A controversial subject Lettera Go to
2018 Anti-PCSK9 treatment: Is ultra-low LDL always good? Articolo in rivista Go to
2018 Identification and diagnosis of patients with familial chylomicronaemia syndrome (FCS): Expert panel recommendations and proposal of an “FCS score” Articolo in rivista Go to
2018 Liver and statins: a critical appraisal of the evidence Articolo in rivista Go to
2018 Lack of Correlation of Plasma HDL With Fecal Cholesterol and Plasma Cholesterol Efflux Capacity Suggests Importance of HDL Functionality in Attenuation of Atherosclerosis Articolo in rivista Go to
2018 Characterisation of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS): Establishment of an FCS clinical diagnostic score Articolo in rivista Go to
2018 Evaluation of the performance of Dutch Lipid Clinic Network score in an Italian FH population: The LIPIGEN study Articolo in rivista Go to
2018 Platelet Count Does Not Predict Bleeding in Cirrhotic Patients: Results from the PRO-LIVER Study Articolo in rivista Go to
2017 Association between familial hypobetalipoproteinemia and the risk of diabetes. Is this the other side of the cholesterol–diabetes connection? A systematic review of literature Articolo in rivista Go to
2017 Differences in cardiac structure and function between black and white patients: Another step in the evaluation of cardiovascular risk in chronic kidney disease Nota o commento Go to
2017 Identification of a novel LMF1 nonsense mutation responsible for severe hypertriglyceridemia by targeted next-generation sequencing Articolo in rivista Go to
2017 Severe reduction of blood lysosomal acid lipase activity in cryptogenic cirrhosis: A nationwide multicentre cohort study Articolo in rivista Go to
2017 How to assess and manage cardiovascular risk associated with lipid alterations beyond LDL Articolo in rivista Go to
2017 Effect of aspirin on renal disease progression in patients with type 2 diabetes: A multicenter, double-blind, placebo-controlled, randomized trial. The renaL disEase progression by aspirin in diabetic pAtients (LEDA) trial. Rationale and study design Articolo in rivista Go to
2017 Threshold Effects of Circulating Angiopoietin-like 3 Levels on Plasma Lipoproteins Articolo in rivista Go to
2017 The role of registries in rare genetic lipid disorders: Review and introduction of the first global registry in lipoprotein lipase deficiency Articolo in rivista Go to
2017 ANMCO/ISS/AMD/ANCE/ARCA/FADOI/GICR-IACPR/SICI-GISE/SIBioC/SIC/SICOA/SID/SIF/SIMEU/SIMG/SIMI/SISA Joint Consensus Document on cholesterol and cardiovascular risk: Diagnostic-therapeutic pathway in Italy Articolo in rivista Go to
2017 Long-term efficacy and safety of the microsomal triglyceride transfer protein inhibitor lomitapide in patients with homozygous familial hypercholesterolemia Lettera Go to
2017 Familial hypercholesterolemia: The Italian Atherosclerosis Society Network (LIPIGEN) Articolo in rivista Go to
2017 Familial hypercholesterolemia: The Italian Atherosclerosis Society Network (LIPIGEN) Articolo in rivista Go to
2017 Clinical and biochemical characteristics of individuals with low cholesterol syndromes: A comparison between familial hypobetalipoproteinemia and familial combined hypolipidemia Articolo in rivista Go to
2017 Cardiovascular efficacy and safety of bococizumab in high-risk patients Articolo in rivista Go to
2017 Efficacy of Lomitapide in the Treatment of Familial Homozygous Hypercholesterolemia: Results of a Real-World Clinical Experience in Italy Articolo in rivista Go to
2017 Atorvastatin but not pravastatin impairs mitochondrial function in human pancreatic islets and rat β-cells. Direct effect of oxidative stress Articolo in rivista Go to
2017 Under-prescription of statins in patients with non-alcoholic fatty liver disease Articolo in rivista Go to
2017 Spectrum of mutations in Italian patients with familial hypercholesterolemia: New results from the LIPIGEN study Articolo in rivista Go to
2017 Genotypic and phenotypic characterization of patients with autosomal dominant hypercholesterolemia in sicily Abstract in atti di convegno pubblicato in rivista Go to
2017 Diagnostic algorithm for familial chylomicronemia syndrome Articolo in rivista Go to
2017 Inverse association between type 2 diabetes and aortic root dimension in hypertensive patients Articolo in rivista Go to
2016 Genetic susceptibility to the coronary artery diseases Capitolo o Saggio Go to
2016 PULMONARY EMBOLISM IN AN EMERGENCY CARE UNIT: EVALUATION OF PREDICTIVE FACTORS FROM CLINICAL HISTORY AND PHYSICAL EXAM Articolo in rivista Go to
2016 Individual analysis of patients with HoFH participating in a phase 3 trial with lomitapide: The Italian cohort Articolo in rivista Go to
2016 Colesterolo e rischio cardiovascolare: Percorso diagnostico-terapeutico in Italia Articolo in rivista Go to
2016 FragClust and TestClust, two informatics tools for chemical structure hierarchical clustering analysis applied to lipidomics. The example of Alzheimer's disease Articolo in rivista Go to
2016 Lomitapide affects HDL composition and function Articolo in rivista Go to
2016 Proprotein Convertase Subtilisin Kexin Type 9 Inhibition for Autosomal Recessive Hypercholesterolemia - Brief Report Articolo in rivista Go to
2016 Efficacy and safety of adding alirocumab to rosuvastatin versus adding ezetimibe or doubling the rosuvastatin dose in high cardiovascular-risk patients: The ODYSSEY OPTIONS II randomized trial Articolo in rivista Go to
2016 Characterization of a mutant form of human apolipoprotein B (Thr26-Tyr27del) associated with familial hypobetalipoproteinemia Articolo in rivista Go to
2016 Baseline metabolic disturbances and the twenty-five years risk of incident cancer in a Mediterranean population Articolo in rivista Go to
2016 Microsomal triglyceride transfer protein gene mutations in Turkish children: A novel mutation and clinical follow up Articolo in rivista Go to
2016 Myristic acid is associated to low plasma HDL cholesterol levels in a Mediterranean population and increases HDL catabolism by enhancing HDL particles trapping to cell surface proteoglycans in a liver hepatoma cell model Articolo in rivista Go to
2016 La diagnostica di laboratorio delle dislipidemie Articolo in rivista Go to
2016 Documento di consenso intersocietario ANMCO/ISS/AMD/ANCE/ARCA/FADOI/ GICR-IACPR/SICI-GISE/SIBioC/SIC/SICOA/ SID/SIF/SIMEU/SIMG/SIMI/SISA Colesterolo e rischio cardiovascolare: percorso diagnostico-terapeutico in Italia Articolo in rivista Go to
2016 Portal vein thrombosis relevance on liver cirrhosis: Italian Venous Thrombotic Events Registry Articolo in rivista Go to
2016 Erratum: FragClust and TestClust, two informatics tools for chemical structure hierarchical clustering analysis applied to lipidomics. The example of Alzheimer's disease (Analytical and Bioanalytical Chemistry DOI: 10.1007/s00216-015-9229-6) Articolo in rivista Go to
2016 Albumin versus solvent/detergent-treated pooled plasma as replacement fluid for long-term plasma exchange therapy in a patient with primary hypertriglyceridemia and recurrent hyperlipidemic pancreatitis Articolo in rivista Go to
2015 Homozygous familial hypobetalipoproteinemia: Two novel mutations in the splicing sites of apolipoprotein B gene and review of the literature Articolo in rivista Go to
2015 Issues Affecting Quality of Life and Disease Burden in Lipoprotein Lipase Deficiency (Lpld) - First Step Towards a Pro Measure in Lpld Proceedings Go to
2015 Heparin induces an accumulation of atherogenic lipoproteins during hemodialysis in normolipidemic end-stage renal disease patients. Articolo in rivista Go to
2015 Efficacy and safety of alirocumab in reducing lipids and cardiovascular events Articolo in rivista Go to
2015 Novel CREB3L3 Nonsense Mutation in a Family With Dominant Hypertriglyceridemia Articolo in rivista Go to
2015 Treating homozygous familial hypercholesterolemia in a real-world setting: Experiences with lomitapide Articolo in rivista Go to
2015 The effect of ezetimibe on NAFLD Articolo in rivista Go to
2015 Familial hypercholesterolæmia in children and adolescents: Gaining decades of life by optimizing detection and treatment Articolo in rivista Go to
2015 Exome sequencing in suspected monogenic dyslipidemias Articolo in rivista Go to
2015 Role of Nutraceuticals in Hypolipidemic Therapy Articolo in rivista Go to
2015 Identifying genetic risk variants for coronary heart disease in familial hypercholesterolemia: an extreme genetics approach Articolo in rivista Go to
2015 Spectrum of mutations of the LPL gene identified in Italy in patients with severe hypertriglyceridemia Articolo in rivista Go to
2015 The pathophysiology of intestinal lipoprotein production Articolo in rivista Go to
2015 The lipid-lowering effects of lomitapide are unaffected by adjunctive apheresis in patients with homozygous familial hypercholesterolaemia - A post-hoc analysis of a Phase 3, single-arm, open-label trial Articolo in rivista Go to
2015 Apolipoprotein AI and HDL are reduced in stable cirrhotic patients with adrenal insufficiency: A possible role in glucocorticoid deficiency Articolo in rivista Go to
2014 RUOLO DEL POLIMORFISMO ILE148MET DEL GENE PNPLA3 NELLA STEATOSI ASSOCIATA ALLA IPOBETALIPOPROTEINEMIA FAMILIARE Proceedings Go to
2014 LA LIPIDOMICA DELLA NON ALCOHOLIC FATTY LIVER DISEASE: ANALISI DELLA CINETICA DELL’ACIDO PALMITICO MEDIANTE L’USO DI UN ISOTOPO STABILE IN UN MODELLO IN VITRO Proceedings Go to
2014 NEXT GENERATION SEQUENCIN: A NEW METHODOLOGICAL APPROACH FOR THE MOLECULAR DIAGNOSIS OF GENETIC DYSLIPIDEMIAS Proceedings Go to
2014 Lomitapide: a novel drug for homozygous familial hypercholesterolemia Articolo in rivista Go to
2014 Oxidative status in metabolic syndrome Proceedings Go to
2014 Beyond Statins: New Lipid Lowering Strategies to Reduce Cardiovascular Risk Articolo in rivista Go to
2014 Lipid Peroxidation, Nitric Oxide Metabolites, and Their Ratio in a Group of Subjects with Metabolic Syndrome Articolo in rivista Go to
2014 DETECTION OF NEW GENES RESPONSIBLE OF FAMILIAL RECESSIVE HYPERCHOLESTEROLEMIA: PRELIMINARY DATA FROM AN EXOME SEQUENCING APPROACH Proceedings Go to
2014 Gelatinases and their tissue inhibitors in metabolic syndrome Proceedings Go to
2014 Behavior of the total antioxidant status in a group of subjects with metabolic syndrome. Articolo in rivista Go to
2014 Clinical experience of lomitapide therapy in patients with homozygous familial hypercholesterolaemia Articolo in rivista Go to
2014 Metabolic mediators of the effects of body-mass index, overweight, and obesity on coronary heart disease and stroke: a pooled analysis of 97 prospective cohorts with 1·8 million participants Articolo in rivista Go to
2014 The use of statins in people at risk of developing diabetes mellitus: Evidence and guidance for clinical practice Articolo in rivista Go to
2014 Homozygous familial hypercholesterolaemia: new insights and guidance for clinicians to improve detection and clinical management. A position paper from the Consensus Panel on Familial Hypercholesterolaemia of the European Atherosclerosis Society Articolo in rivista Go to
2014 Nuove linee guida americane 2013 ACC/AHA sul trattamento del colesterolo plasmatico per ridurre il rischio cardiovascolare aterosclerotico: confronto con le raccomandazioni ESC/EAS per la gestione delle dislipidemie Articolo in rivista Go to
2014 eNOS activation by HDL is impaired in genetic CETP deficiency Articolo in rivista Go to
2014 Study of the Correlations among Some Parameters of the Oxidative Status, Gelatinases, and Their Inhibitors in a Group of Subjects with Metabolic Syndrome Articolo in rivista Go to
2013 Clinical characteristics and plasma lipids in subjects with familial combined hypolipidemia: a pooled analysis Articolo in rivista Go to
2013 Familial hypercholesterolaemia is underdiagnosed and undertreated in the general population: guidance for clinicians to prevent coronary heart disease: Consensus Statement of the European Atherosclerosis Society Articolo in rivista Go to
2013 LINEE GUIDA CLINICHE PER LA PREVENZIONE DELLA CARDIOPATIA ISCHEMICA NELLA IPERCOLESTEROLEMIA FAMILIARE Una patologia sotto-diagnosticata e sotto-trattata Articolo in rivista Go to
2013 Spectrum of mutations and phenotypic expression in patients with autosomal dominant hypercholesterolemia identified in Italy Articolo in rivista Go to
2013 OLESTEROLO: UNA MOLECOLA "MOLTO CONTROLLATA" Recensione in rivista Go to
2013 A Novel APOB Mutation Identified by Exome Sequencing Cosegregates With Steatosis, Liver Cancer, and Hypocholesterolemia. Articolo in rivista Go to
2013 Nonalcoholic fatty liver and metabolic syndrome in Italy: Results from a multicentric study of the Italian Arteriosclerosis society Articolo in rivista Go to
2013 Protein oxidation in a group of subjects with metabolic syndrome. Articolo in rivista Go to
2013 Oxidative status in nondiabetic middle-aged subjects with metabolic syndrome: preliminary data. Articolo in rivista Go to
2013 Efficacy and Safety of Ezetimibe Added to Atorvastatin Versus Atorvastatin Uptitration or Switching to Rosuvastatin in Patients With Primary Hypercholesterolemia Articolo in rivista Go to
2013 Familial combined hypolipidemia due to mutations in the ANGPTL3 gene Articolo in rivista Go to
2013 Gelatinases and their tissue inhibitors in a group of subjects with metabolic syndrome Articolo in rivista Go to
2013 REDUCTION OF CHOLESTEROL WITH NUTRACEUTICAL: RESULTS OF A DOUBLE BLIND STUDY Proceedings Go to
2013 CLINICAL CHARACTERISTICS AND PLASMA LIPIDS IN SUBJECTS WITH FAMILIAL COMBINED HYPOLIPIDEMIA: A POOLED ANALYSIS Proceedings Go to
2013 LIPIDOMICS OF HUMAN SKIN FIBROBLASTS IN NEIMANN-PICK DISEASE TYPE C Proceedings Go to
2013 FUNCTIONAL CHARACTERIZATION OF NOVEL AMINO ACID VARIANTS IN APOB IN FAMILIAL HYPOBETALIPOPROTEINEMIA Proceedings Go to
2013 A NOVEL APOB MUTATION IDENTIFIED BY EXOME SEQUENCING COSEGREGATES WITH STEATOSIS, LIVER CANCER AND HYPOCHOLESTEROLEMIA Proceedings Go to
2013 Enhanced Lipid Peroxidation and Platelet Activation as Potential Contributors to Increased Cardiovascular Risk in the Low-HDL Phenotype Articolo in rivista Go to
2013 The Atrial Natriuretic Peptide Genetic Variant Rs5068 Is Associated With a Favorable Cardiometabolic Phenotype in a Mediterranean Population Articolo in rivista Go to
2013 Efficacy and safety of a microsomal triglyceride transfer protein inhibitor in patients with homozygous familial hypercholesterolaemia: a single-arm, open-label, phase 3 study Articolo in rivista Go to
2013 The polygenic nature of hypertriglyceridaemia: implications for definition, diagnosis, and management. Articolo in rivista Go to
2012 Statin therapy in patients with aortic stenosis after the ASTRONOMER trial: is there still any space? Articolo in rivista Go to
2012 IL PROGETTO LIPIGEN: UN AGGIORNAMENTO Articolo in rivista Go to
2012 Prothrombotic gene variants as risk factors of acute myocardial infarction in young women. Articolo in rivista Go to
2012 Evaluation of nitric oxide metabolites in a group of subjects with metabolic syndrome. Articolo in rivista Go to
2012 Lipid-Altering Efficacy of Ezetimibe/Simvastatin 10/20 mg Compared to Rosuvastatin 10 mg in High-Risk Patients with and without Type 2 Diabetes Mellitus Inadequately Controlled Despite Prior Statin Monotherapy. Articolo in rivista Go to
2012 Prothrombotic gene variants in AMI young women Proceedings Go to
2012 Clinical utility of novel biomarkers for cardiovascular disease risk stratification Articolo in rivista Go to
2012 Prediction of incident type 2 diabetes mellitus based on a twenty-year follow-up of the Ventimiglia heart study Articolo in rivista Go to
2012 Lipid and apoprotein composition of HDL in partial or complete CETP deficiency Articolo in rivista Go to
2012 Identification of a novel ANGPTL3 mutation splicing associeted to severe hypobetalipoproteinemia Proceedings Go to
2012 Clinical, molecular and functional characterization of two novel mutations associated to compound heterozygous FHBL Proceedings Go to
2012 Prevalence of ANGPTL3 and APOB gene mutations in subjects with combined hypolipidemia Articolo in rivista Go to
2012 The ANP Genetic Variant RS5068 is Associated With a Favorable Cardiometabolic Phenotype in a Mediterranean Population Proceedings Go to
2011 Hypobetalipoproteinemia: genetics, biochemistry, and clinical spectrum. Articolo in rivista Go to
2011 SWITCHING FROM STATIN MONOTHERAPY TO EZETIMIBE/SIMVASTATIN OR ROSUVASTATIN MODIFIES THE RELATIONSHIPS BETWEEN APOLIPOPROTEIN B, LDL CHOLESTEROL, ANC NON-HDL CHOLETEROL IN PATIENTS AT HIGH RISK OF CORONARY DISEASE Articolo in rivista Go to
2011 Identification of a novel mutation of MTP gene in a patient with abetalipoproteinemia. Articolo in rivista Go to
2011 Le Dislipidemie Genetiche. Il Progetto LIPIGEN Articolo in rivista Go to
2011 PREVALENCE OF 'BORDERLINE' VALUES OF CARDIOVASCULAR RISK FACTORS IN THE CLINICAL PRACTICE OF GENERAL MEDICINE IN ITALY: RESULTS OF THE BORDERLINE STUDY. Articolo in rivista Go to
2011 Lipid-altering efficacy of switching to ezetimibe/simvastatin 10/20 mg versus rosuvastatin 10 mg in high-risk patients with and without metabolic syndrome Articolo in rivista Go to
2011 Plasma non-cholesterol sterols in primary hypobetalipoproteinemia Articolo in rivista Go to
2011 A genetic variant of the atrial natriuretic peptide gene is associated with cardiometabolic protection in the general community Articolo in rivista Go to
2011 PREVALENCE OF ANGPTL3 AND APOB GENE MUTATIONS IN SUBJECTS WITH COMBINED HYPOLIPIDEMIA Proceedings Go to
2011 FUNCTIONAL EFFECT OF NOVEL AMINO ACID VARIANTS OF APOLIPOPROTEIN B IN FAMILIAL HYPOBETALIPOPROTEINEMIA Proceedings Go to
2011 VASCULOPROTECTIVE FUNCTION OF HDL FROM CETP-DEFICIENT SUBJECTS Proceedings Go to
2011 LIPIDOMICS OF FATTY LIVER IN NAFLD AND HCV INFECTION: LIVER SPHYNGOLIPIDS AND FATTY ACIDS Proceedings Go to
2011 Metabolomic analysis of plasma from Alzheimer disease patients Proceedings Go to
2011 LIPASE MATURATION FACTOR 1 IS REQUIRED FOR ENDOTHELIAL LIPASE ACTIVITY Articolo in rivista Go to
2010 Il paziente con SCA dopo dimissione dall'ospedale: terapia di mantenimento con statine Articolo in rivista Go to
2010 Effects of PCSK9 variants on common carotid artery intima media thickness and relation to ApoE alleles. Articolo in rivista Go to
2010 Paziente con obesità viscelare, asintomatico Articolo in rivista Go to
2010 Ezetimibe/Simvastatin 10/20 mg versus Rosuvastatin 10 mg in high-risk hypercholesterolemic patients stratified by prior statin treatment potency. Articolo in rivista Go to
2010 The production of 85 kDa N-terminal fragment of apolipoprotein B in mutant HepG2 cells generated by targeted modification of apoB gene occurs by ALLN-inhibitable protease cleavage during translocation. Articolo in rivista Go to
2010 Postprandial hyperglycemia is a determinant of platelet activation in early type 2 diabetes mellitus. Articolo in rivista Go to
2010 Compliance al trattamento in un paziente in terapia ipocolesterlemizzante Articolo in rivista Go to
2010 A novel component of the metabolic syndrome : The oxidative stress Articolo in rivista Go to
2010 Variable phenotypic expression of chylomicron retention disease in a kindred carrying a mutation of the Sara2 gene Articolo in rivista Go to
2010 Modification of the lipidic and coagulative pattern in postmenopause women: effect of hormone replacement therapy. Articolo in rivista Go to
2010 A novel putative interactor for the low density lipoprotein receptor cytoplasmic domain Articolo in rivista Go to
2010 Plasma non-cholesterol sterols: a useful diagnostic tool in pediatric hypercholesterolemia. Articolo in rivista Go to
2010 Ezetimibe/simvastatin 10/20 mg versus simvastatin 40 mg in coronary heart disease patients Articolo in rivista Go to
2010 POSTPRANDIAL HYPERGLYCEMIA IS A DETERMINANT OF PLATELET ACTIVATION IN EARLY 2 DIABETES MELLITUS Articolo in rivista Go to
2009 Obesity and the metabolic syndrome in a student cohort from Southern Italy Articolo in rivista Go to
2009 C-reactive protein but not soluble CD40 ligand and homocysteine is associated to common atherosclerotic risk factors in a cohort of coronary artery disease patients. Articolo in rivista Go to
2009 Marker dell'infiammazione : quali le implicazioni degli studi più recenti? Articolo in rivista Go to
2009 La supplementazione con substrati pro-energetivi nel soggetto astenico Articolo in rivista Go to
2009 Effects of a phytosterol-enriched dairy product on lipids, sterols and 8-isoprostane in hypercholesterolemic patients: A multicenter Italian study. Articolo in rivista Go to
2009 Down regulation of CD11b and CD18 expression in children with hypercholesterolemia: A preliminary report. Articolo in rivista Go to
2009 Paziente con infarto miocardico, bassa colesterolemia e aumentali livelli PCR Articolo in rivista Go to
2009 Novel LMF1 nonsense mutation in a patient with severe hypertriglyceridemia Articolo in rivista Go to
2009 Familial hypobetalipoproteinemia due to apolipoprotein B R463W mutation causes intestinal fat accumulation and low postprandial lipemia. Articolo in rivista Go to
2009 Il paziente anziano Articolo in rivista Go to
2009 Dislipidemia della sindrome metabolica . fisiopatologia e clinica Articolo in rivista Go to
2009 Lipid-altering efficacy of ezetimibe/simvastatin 10/20 mg compared with rosuvastatin 10 mg in high-risk hypercholesterolaemic patients inadequately controlled with prior statin monotherapy - The IN-CROSS study. Articolo in rivista Go to
2009 Hypertension and diabetes mellitus are associated with cardiovascular events in the elderly without cardiovascular disease. Results of a 15-year follow-up in a Mediterranean population Articolo in rivista Go to
2009 Novel mutations of CETP gene in Italian subjects with hyeralphalipoproteinemia Articolo in rivista Go to
2008 A novel mutation in the Lipase Maturaction Factor 1 (LMF-1)gene responsible for severe hypertriglyceridemia Proceedings Go to
2008 PATIENT PROFILE: UN PAZIENTE CON FENOTIPO LIPOPROTEICO ATEROGENO Articolo in rivista Go to
2008 The metabolic syndrome predicts cardiovascular events in subjects with normal fasting glucose: Results of a 15 years follow-up in a Mediterranean population. Articolo in rivista Go to
2008 Paziente donna a elevatissimo rischio cardiovascolare Abstract in rivista Go to
2008 Lo studio Corona: un commento Articolo in rivista Go to
2008 Clinical, pathologic, and genetic features of massive soft tissue neurofibromas in a Sicilian patient Articolo in rivista Go to
2008 Dietary cholesterol and estrogen administration elevate brain apolipoprotein E in mice by different mechanisms Articolo in rivista Go to
2007 Interleukin 6 plasma levels predict with high sensitivity and specificity coronary stenosis detected by coronary angiography Articolo in rivista Go to
2007 CARDIOVASCULAR RISK FACTORS ANALYSIS OF PEDIATRIC MATABOLIC SYNDROME Proceedings Go to
2007 Decreased plasma soluble RAGE in patients with hypercholesterolemia: Effects of statins Articolo in rivista Go to
2007 INTERLEUKIN 6 PLASMA LEVELS PREDICT WITH HIGH SENSITIVITY AND SPECIFICITY CORONARY STENOSIS DETECTED BY CORONARY ANGIOGRAPHY Proceedings Go to
2007 GENETIC HETEROGENEITY OF SEVERE HYPOBETALIPOPROTEINEMIA Proceedings Go to
2007 TERAPIA CON STATINE IN PAZIENTI SICILIANI AFFETTI DA IPERLIPIDEMIA FAMILIARE COMBINATA Articolo in rivista Go to
2007 EZETIMIBE: QUALE RUOLO ALLA LUCE DELLE NUOVE LINEE GUIDA? Articolo in rivista Go to
2007 FAMILIAL HYPOBETALIPOPROTEINEMIA DUE TO APOLIPOPROTEIN B GENE MUTATIONS CAUSES INTESTINAL FAT ACCUMULATION AND LIPID MALABSORPTION. Proceedings Go to
2007 THE METABOLIC SYNDROME PREDICTS CARDIOVASCULAR EVENTS IN SUBJECTS WITH NORMAL FASTING GLUCOSE. A FIFTEEN YEARS FOLLOW-UP IN A MEDITERRANEAN POPULATION Proceedings Go to
2007 MUTATIONS IN THE CETP GENE IN ITALIAN SUBJECTS WITH HYPERALPHALIPOPROTEINEMIA Proceedings Go to
2007 INTERACTION OF THE INTRACELLULAR DOMAIN OF THE LOW DENSITY LIPOPROTEIN (LDL) RECPTOR WITH METALLOTHIONEIN2 (MT2). Proceedings Go to
2007 Genetics of familial hypobetalipoproteinemia Articolo in rivista Go to
2007 A NOVEL LOSS OF FUCTION MUTATION OF PCSK9 GENE IN CAUCASIANS WITH LOW PLASMA LDL-CHOLESTEROL Proceedings Go to
2007 ΒETA ARRESTIN-2: A NEW “ACTOR” IN THE LDL-R ENDOCYTOSIS? Proceedings Go to
2007 LE IPERCOLESTEROLEMIE PRIMITIVE Articolo in rivista Go to
2007 HYPERTENSION AND DIABETES MELLITUS PREDICT CARDIOVASCULAR EVENTS IN ELDERLY WITHOUT CARDIOVASCULARDISEASE. RESULTS OF FIFTEEN YEARS FOLLOW-UP IN A MEDITERRANEAN POPULATION. Proceedings Go to
2007 CLINICAL AND MOLECULAR CHARACTERIZATION OF HYPERCHOLESTEROLEMIC SICILIAN FAMILIES AND DESCRIPTION OF 3 NOVEL MUTATIONS IN THE LDLR GENE Proceedings Go to
2007 PATIENT PROFILE: PAZIENTE AD ALTISSIMO RISCHIO CARDIOVASCOLARE CON ADERENZA INSUFFICIENTE ALLA TERAPIA Articolo in rivista Go to
2007 IL GENE PCSK9: UN NUOVO GENE IMPLICATO NEL CONTROLLO DELLA COLESTEROLEMIA Articolo in rivista Go to
2007 A metallothionein family member interacts with the intracellular domain of the low density lipoprotein (ldl) receptor. Proceedings Go to
2007 EFFECT OF THE 420C/G VARIANT OF THE RESISTIN GENE PROMOTER ON METABOLIC SYNDROME, OBESITY, MYOCARDIAL INFARCTION AND RENAL DYSFUNCTION Articolo in rivista Go to
2007 SHORT APOB TRUNCATIONS SHOW IMPAIRE CHYLOMICRON EXPORT AND ENTEROCYTE TRIGLYCERIDE ACCUMULATION. IN VIVO AND IN VITRO EVIDENCE ON A APOB 28.25 STABLE-TRANSFECTED ENTEROCYTE CELL LINE Proceedings Go to
2007 NUOVE DISPOSIZIONI DELLA NOTA 13 PER PAZIENTI HIV-POSITIVI IN TERAPIA ANTIRETROVIALE E PER PAZIENTI CON INSUFFICIENZA RENALE CRONICA Articolo in rivista Go to
2007 Molecular diagnosis of hypobetalipoproteinemia: An ENID review Articolo in rivista Go to
2007 A novel loss of function mutation of PCSK9 gene in white subjects with low-plasma low-density lipoprotein cholesterol. Articolo in rivista Go to
2006 Low-density lipoproteins generated during an oral fat load in mild hypertriglyceridemic and healthy subjects are smaller, denser, and have an increased low-density lipoprotein receptor binding affinity. Articolo in rivista Go to
2006 Association between apolipoprotein E epsilon4 allele and apathy in probable Alzheimer's disease. Articolo in rivista Go to
2006 Unexpleined elevated serum pancreatic enzymes: a reason to suspect celiac disease Articolo in rivista Go to
2006 CETP levels rather than polymorphisms as markers of coronary risk: healthy athlete with high HDL-C and coronary disease--effectiveness of probucol. Articolo in rivista Go to
2006 Analysis of sterols by high-performance liquid chromatography/mass spectrometry combined with chemometrics Articolo in rivista Go to
2006 THE METABOLIC SYNDROME PREDICTS CARDIOVASCULAR EVENTS IN SUBJECTS WITH NORMAL GLUCOSE TOLERANCE. A 15 YEARS FOLLOW-UP IN A MEDITERRANEAN POPULATION Proceedings Go to
2006 EZETIMIBE: WHAT ROLE in the light of recent guidelines Articolo in rivista Go to
2006 COMPOUND HETEROZYGOUS FH AND FDB: IDENTIFICATION OF A SICILIAN FAMILY HARBOURING THE FDB3531 MUTATION AND THE Y398X MUTATION OF THE LDL RECEPTOR GENE. Proceedings Go to
2006 A Novel Liquid Chromatography/Mass Spectrometry Method for Analysis of Plasma Sterol Concentrations Proceedings Go to
2006 CLINICAL AND RESEARCH CONCEPTS: GENETICA DELLE DISLIPIDEMIE (LE IPERCOLESTEROLEMIE) Articolo in rivista Go to
2006 RT-PCR and in situ hybridization analysis of apolipoprotein H expression in rat normal tissues Articolo in rivista Go to
2006 Multiple food hypersensitivity as a cause of refractory chronic constipation in adults Articolo in rivista Go to
2006 L’uso di stent con sirolimus e’ significativamente associate alla riduzione della mortalita’ totale e della morbidita’ cardiovascolare sia a 6 mesi che a 12 mesi post-PTCA. Abstract in rivista Go to
2006 VARIABLE PHENOTYPIC ESPRESSION IN A LIPID ABSORPTION DISORDER DUE TO A MOLECULAR DEFECT IN THE SARA2 GENE Proceedings Go to
2006 A NOVEL NONSENSE MUTATION IN THE CETP GENE IN ITALIAN HYPERALPHALIPOPROTEINEMIC SUBJECTS Proceedings Go to
2006 Additive effect of mutations in LDLR and PCSK9 genes on the phenotyoe of familial hypercholesterolemia Articolo in rivista Go to
2006 PREVALENCE OF PCSK9 VARIANTS IN A COHORT OF SUBJECTS WITH HYPOCHOLESTEROLEMIA Proceedings Go to
2006 Six novel mutations of the LDL receptor gene in FH kindred of Sicilian and Paraguayan descent Articolo in rivista Go to
2006 PATIENT PROFILE: PAZIENTE NEFROPATICO, PAZIENTE GIOVANE CON DIABETE, PAZIENTE DONNA, PAZIENTE IN ETÀ pediatrica Articolo in rivista Go to
2006 PREVALENCE OF A METABOLIC SYNDROME AMONG A PEDIATRIC CASISTIC FROM THE MOUNTAIN COMMUNITY (SERRE CALABRE). Proceedings Go to
2006 Use of stents with sirolimus is significantly associated with a reduction in mortality and cardiovascular morbidity at 6- and 12-months post-PTCA Abstract in rivista Go to
2006 ENHANCED LIPID PEROXIDATION AND PLATELET ACTIVATION AS POTENTIAL CONTRIBUTORS TO INCREASED CARDIOVASCULAR RISK IN THE LOW-HDL PHENOTYPE. Proceedings Go to
2006 A NOVEL LOSS OF FUNCTION MUTATION OF PCSK9 GENE Proceedings Go to
2006 CLINICAL AND RESEARCH CONCEPTS: LE BARRIERE LEGATE AL PAZIENTE Articolo in rivista Go to
2006 Gene expression in mouse spermatogenesis during ontogenesis. Articolo in rivista Go to
2006 Association of estrogen receptor alpha gene with Alzheimer's disease: a case-control study Articolo in rivista Go to
2006 A Targeted ApoB38.9 Mutation in Mice Is Associated with Reduced Hepatic Cholesterol Synthesis and Enhanced Lipid Peroxidation. Articolo in rivista Go to
2006 The c.43_44insCTG variation in PCSK9 is associated with low plasma LDL-cholesterol in a Caucasian population. Articolo in rivista Go to
2006 CEREBROTENDINOUS XANTHOMATOSIS: A SICILIAN FAMILY HARBOURING THE R362C MUTATION IN THE STEROL 27-HYDROXYLASE GENE Proceedings Go to
2006 Accumulation of apoE-enriched triglyceride-rich lipoproteins in patients with coronary artery disease Articolo in rivista Go to
2005 HYPOBETALIPOPROTEINEMIA AND FATTY LIVER: WHO IS THE CULPRIT Proceedings Go to
2005 No association between the cystatin C gene polymorphism and Alzheimer's disease: a case-control study in an Italian population. Articolo in rivista Go to
2005 Cystatin C levels are decreased in acute myocardial infarction: Effect of cystatin C G73A gene polymorphism on plasma levels Articolo in rivista Go to
2005 Family hystory, diabetes and extension of coronary atherosclerosis are strong predictors of adverse events after PTCA: a one year follow-up study Articolo in rivista Go to
2005 PREVALENCE OF APOB VARIANTS IN A SAMPLE OF SUBJECTS WITH HYPOCHOLESTEROLEMIA Proceedings Go to
2005 THERAPEUTIC LIFESTYLE CHANGES: L’ALIMENTAZIONE Articolo in rivista Go to
2005 Chronic constipation and food intolerance: a model of proctitis causing constipation Articolo in rivista Go to
2005 DIFFERENCE IN THE PREVALENCE OF METABOLIC SYNDROME AND CARDIOVASCULAR RISK FACTORS AFTER 14 YEARS IN THE POPULATION OF VENTIMIGLIA DI SICILIA Proceedings Go to
2005 Anti-actin antibodies in celiac disease: correlation with intestinal mucosa damage and comparison of ELISA with the immunofluorescence assay. Articolo in rivista Go to
2005 A Novel Mutation of the DHCR7 Gene in a Sicilian Compound Heterozygote with Smith-Lemli-Opitz Syndrome Articolo in rivista Go to
2005 A novel mutation of the extracellular matrix protein 1 gene (ECM1) in a patient with lipoid proteinosis (Urbach-Wiethe disease) from Sicily Articolo in rivista Go to
2005 ENHANCED LIPID PEROXIDATION AND PLATELET ACTIVATION AS POTENTIAL CONTRIBUTORS TO INCREASED CARDIOVASCULAR RISK IN THE “LOW-HDL” PHENOTYPE. Proceedings Go to
2005 Relazione tra il size delle LDL e l’estensione della malattia vasale coronarica in 72 pazienti maschi sottoposti a coronarografia diagnostica Abstract in rivista Go to
2005 GASTROINTESTINAL SYMPTOMS IN INFANCY: A POPULATION-BASED PROSPECTIVE STUDY Articolo in rivista Go to
2005 CLINICAL AND RESEARCH CONCEPTS: NUTRIZIONE E METABOLISMO Articolo in rivista Go to
2005 FAMILIAL HYPOALPHALIPOPROTEINEMIA ASSOCIATED TO CORNEAL OPACITIES IN ABSENCE OF LCAT DEFICIENCY Proceedings Go to
2005 SEVERE MALABSORPTION AND DECREASED TRIGLYCERIDE RICH LIPOPROTEINS PRODUCTION IN A PROBAND CARRYING A MUTATION ENCODING FOR A TRUNCATED APOLIPOPROTEIN B100 VARIANT (APO B 34.8). Proceedings Go to
2005 A NOVEL COMPOUND HETEROZYGOUS MUTATION OF THE LIPOPROTEIN LIPASE GENE IN A NEWBORN WITH CHYLOMICRONEMIA Proceedings Go to
2005 MUSCLE DAMAGE AND PAIN IN HYPERCHOLESTEROLEMIC OUT-PATIENTS POPULATION ON STATIN TREATMENT. Proceedings Go to
2005 Drug eluting stents's use in patients with anatomical or clinical patterns favouring restenosis: a 6-months follow-up study Proceedings Go to
2005 Bovine seminal ribonuclease is cytotoxic for both malignant and normal telomerase-positive cells Articolo in rivista Go to
2005 ADDITIVE EFFECT OF MUTATIONS IN LDLR AND PCSK9 GENES ON THE PHENOTYPE OF FAMILIAL HYPERCHOLESTEROLEMIA. Abstract in atti di convegno pubblicato in volume Go to
2005 Drug eluting stents's use in patients with anatomical or clinical patterns favouring restenosis: a 6-months follow-up study. Atherosclerosis. 2005. 6(suppl.1) Proceedings Go to
2005 IDENTIFICATION OF A HETEROZYGOUS COMPOUND INDIVIDUAL WITH AUTOSOMAL DOMINANT HYPERCHOLESTEROLEMIA HARBOURING IN THE LDL-R GENE AND IN THE PCSK9 GENE Proceedings Go to
2005 THE METABOLIC SYNDROME IS A PREDICTOR OF CARDIOVASCULAR EVENTS IN A SICILIAN POPULATION. RESULT OF A 15 YEARS FOLLOW UP Proceedings Go to
2005 Mutations in MTP gene in abeta- and hypobeta-lipoproteinemia. Articolo in rivista Go to
2004 Genetic polymorphisms affecting the phenotypic expression of familial hypercholesterolemia Articolo in rivista Go to
2004 FAMILIAL HDL DEFICIENCY DUE TO ABCA1 GENE MUTATIONS WITH OR WITHOUT OTHER GENETIC LIPOPROTEIN DISORDERS Articolo in rivista Go to
2004 A polymorphism in the cyclooxygenase 2 gene as an inherited protective factor against myocardial infarction and stroke Articolo in rivista Go to
2004 ASSOCIATION OF THE PARAOXONASE-1 Q192R POLYMORPHISM WITH CORONARY ARTERY DISEASE IN AMI PATIENTS, NON AMI CAD AND HEALTHY CONTROLS. Proceedings Go to
2004 IDENTIFICATION OF A HETEROZYGOUS COMPOUND INDIVIDUAL WITH AUTOSOMAL DOMINANT HYPERCHOLESTEROLEMIA HARBOURING A MUTATION IN THE LDL-R GENE AND IN THE PCSK9 GENE Proceedings Go to
2004 Transient chylomicronemia preceding the onset of insulin-dependent diabetes in a young girl with no humoral markers of islet autoimmunity. Articolo in rivista Go to
2004 GLI ACIDI GRASSI SATURI ED INSATURI MODULANO L’UPTAKE DELLE LIPOPROTEINE HDL IN UN MODELLO DI CELLULE EPATICHE IN COLTURA. Proceedings Go to
2004 Risultati del follow-up di 6 mesi in 100 pazienti con stent medicato con rapamicina rispetto ad altri 100 con stent tradizionale Abstract in rivista Go to
2004 USE OF THE DRUG ELUTING STENTS WITH RAPAMICIN IN PATIENTS WITH ANATOMICAL OR CLINICAL PATTERNS FAVOURING RESTENOSIS: RESULTS OF A 6-MONTHS FOLLOW-UP ON THE FIRST 100 PATIENS. Proceedings Go to
2004 AN HPLC/APCI METHOD, USING PARTLY MISCIBLE SOLVENTS, FOR A SIMPLE SEPARATION AND DETERMINATION OF STEROLS IN BLOOD Proceedings Go to
2004 UNA NUOVA MUTAZIONE DELL’INTRONE 16 (G>A a 2390 -1) DEL RECETTORE DELLE LDL RESPONSABILE DI IPERCOLESTEROLEMIA FAMILIARE. EFFETTI SULLA ESPRESSIONE DELL’mRNA DEL RECETTORE DELLE LDL Proceedings Go to
2004 Genetic risk factors in myocardial infarction at young age. Articolo in rivista Go to
2004 LDL peak particle size and the extension of coronary atherosclerosis in 72 patients that underwent an angiographic exam Proceedings Go to
2004 Genetic risk factors in myocardial infarction at young age. Minerva Cardioangiol. 2004 Aug;52(4):287-312 Articolo in rivista Go to
2004 A novel nonsense mutation in the cept gene in italian Hyperalphalipoproteinemic subjects Proceedings Go to
2004 HETEROGENITY OF AUTOSOMAL DOMINANT HYPERCHOLESTEROLEMIA IN SICILY Proceedings Go to
2004 BETA-2-GLYCOPROTEIN I IS GROWTH REGULATED AND PLAYS A ROLE AS SURVIVAL FACTOR FOR HEPATOCYTES Articolo in rivista Go to
2004 MALABSORPTION OF FAT IN CELIAC DISEASE DURING AN ORAL FAT LOAD. KINETIC STUDY OF CHYLOMICRONS AND REMNANTS AND CORRELATION WITH THE STAGE OF THE DISEASE Proceedings Go to
2004 ASSOCIAZIONE DEL POLIMORFISMO Q192R DEL GENE DELLA PARAOXONASI I (PON1) CON LA MALATTIA CORONARICA IN UN CAMPIONE DI PZ CON INFARTO MIOCARDICO, MALATTIA CORONARICA NON INFARTUALE E SOGGETTI NORMALI. Proceedings Go to
2004 I LIVELLI DI CISTATINA C SONO RIDOTTI NELL’INFARTO MIOCARDIO ACUTO. EFFETTO DEL POLIMORFISMO G73A SUI LIVELLI PLASMATICI. Proceedings Go to
2004 FAMILIAL LIGAND-DEFECTIVE APOLIPOPROTEIN B: IDENTIFICATION OF A FAMILY HARBOURING THE ARG3531CYS (FDB3531) OF THE APOB GENE Proceedings Go to
2004 Use of the drug eluting stents with rapamicin in patients with anatomical or clinical patterns favouring restenosis: results of a 6-months follow-up on the first 100 patients Abstract in rivista Go to
2004 MISSENSE MUTATION ALA34VAL IN EXON 2 OF THE LIPOPROTEIN LIPASE GENE IN A YOUNG MAN WITH CHYLOMICRONEMIA. Proceedings Go to
2004 IPERCOLESTEROLEMIA AUTOSOMICA DOMINANTE IN SICILIA Proceedings Go to
2004 Le LDL generate in fase post-prandiale dopo carico grasso presentano maggiore densita’, minore size e maggiore affinita’ per il recettore Abstract in rivista Go to
2004 NONSENSE MUTATION IN THE CETP GENE IN ITALIAN HYPERALPHALIPOPROTEINEMIC SUBJECTS. Proceedings Go to
2004 PREVALENCE OF METABOLIC SYNDROME IN A RURAL SICILIAN POPULATION AND RELATIONS WITH CLINICAL EVENTS: THE VENTIMIGLIA HEART PROJECT. Proceedings Go to
2004 MUTAZIONI DEL GENE DELL’APOB RESPONSABILI DI IPOBETALIPOPROTEINEMIA FAMILIARE IN SICILIA Proceedings Go to
2003 Autosomal recessive hypercholesterolemia in a Sicilian kindred harboring the 432insA mutation of the ARH gene. Articolo in rivista Go to
2003 Differential apolipoprotein(a) isoform expression in heterozygosity is an independent contributor to lipoprotein(a) levels variability Articolo in rivista Go to
2003 Autoimmune enteropathy and colitis in an adult patient Articolo in rivista Go to
2003 Screening for celiac disease in non-Hodgkin's lymphoma patients: a serum anti-transglutaminase-based approach Articolo in rivista Go to
2003 Fatty liver in familial hypobetalipoproteinemia: Triglyceride assembly into VLDL particles is affected by the extent of hepatic steatosis Articolo in rivista Go to
2003 Low-density-lipoprotein peak particle size in a Mediterranean population. Articolo in rivista Go to
2003 Diagnostic accuracy of fecal calprotectin assay in distinguishing organic causes of chronic diarrhea from irritable bowel syndrome: a prospective study in adults and children Articolo in rivista Go to
2003 The C(-260)>T gene polymorphism in the promoter of the CD14 monocyte receptor gene is not associated with acute myocardial infarction Articolo in rivista Go to
2003 Association between HFE mutations and acute myocardial infarction: a study in patients from Northern and Southern Italy Articolo in rivista Go to
2003 No association between Glu298Asp endothelial nitric oxide synthase polymorphism and Italian sporadic Alzheimer's disease Articolo in rivista Go to
2003 Two Italian kindreds carrying the Arg136-->Ser mutation of the Apo E gene: development of premature and severe atherosclerosis in the presence of epsilon 2 as second allele Articolo in rivista Go to
2002 Distribution of risk factors, plasma lipids, lipoproteins and dyslipidemias in a small Mediterranean island: the Ustica Project Articolo in rivista Go to
2002 Replication of linkage of familial hypobetalipoproteinemia to chromosome 3p in six kindreds Articolo in rivista Go to
2002 Lack of association between angiotensin converting enzyme polymorphism and sporadic Alzheimer's disease Articolo in rivista Go to
2002 Nutritional characteristics of a rural Southern Italy population: the Ventimiglia di Sicilia Project Articolo in rivista Go to
2002 Comparison of anti-transglutaminase ELISAs and an anti-endomysial antibody assay in the diagnosis of celiac disease: A prospective study Articolo in rivista Go to
2002 Changes in plasma lipids and low-density lipoprotein peak particle size during and after acute myocardial infarction Articolo in rivista Go to
2002 Factor VII activity is an independent predictor of cardiovascular mortality in elderly women of a Sicilian population: Results of an 11-year follow-up Articolo in rivista Go to
2001 ApoE polymorphism in a small Mediterranean island: Relationships with plasma lipids, lipoproteins and LDL particle size Articolo in rivista Go to
2001 Dietary cholate increases plasma levels of apolipoprotein B in mice by posttranscriptional mechanisms Articolo in rivista Go to
2001 Italian familial defective apolipoprotein B patients share a unique haplotype with other Caucasian patients Articolo in rivista Go to
2001 Effectiveness of screening for known mutations in Sicilian patients with "probable" familial hypercholesterolemia Articolo in rivista Go to
2001 Estrogen increases hepatic lipase levels in inbred strains of mice: A possible mechanism for estrogen-dependent lowering of high density lipoprotein Articolo in rivista Go to
2001 Determinants of enhanced thromboxane biosynthesis in renal transplantation Articolo in rivista Go to
2001 Prevalence of overweight and obesity in a rural southern Italy population and relationships with total and cardiovascular mortality: The Ventimiglia di Sicilia project Articolo in rivista Go to
2001 Leukocyte count, diabetes mellitus and age are strong predictors of stroke in a rural population in southern Italy: An 8-year follow-up Articolo in rivista Go to
2001 Carotid atherosclerosis in hypercholesterolemic patients: Relationship with cardiovascular events Articolo in rivista Go to
1999 Lipoprotein(a) levels in relation to albumin concentration in childhood nephrotic syndrome Articolo in rivista Go to
1996 HDL subfractions distribution in renal transplant recipients: Lack of evidence of a reduction of HDL2 particles Articolo in rivista Go to
1996 A new apolipoprotein B truncation (apo B-43.7) in familial hypobetalipoproteinemia: Genetic and metabolic studies Articolo in rivista Go to
1995 Plasma levels of lipoproteins and apolipoproteins in congenital hypothyroidism: effects of L-thyroxine substitution therapy Articolo in rivista Go to